Background
Women with epilepsy (WWE) are considered to be at a high risk of complications during pregnancy [1], although previous research has not shown a substantial increase of seizure burden during pregnancy [2, 3]. Higher incidence of vaginal bleeding, pre-eclampsia, caesarean section, and premature delivery was observed in most WWE compared to the non-epileptic group [4‐6], while some studies found no increased perinatal and neonatal complications [7‐10] . In addition, there is a higher rate of major congenital malformation in babies of WWE, which is most likely related to the prenatal exposure to anti-seizure medications (ASM) [11‐15].
Advanced maternal age is defined as childbearing in a woman aged 35 or older, raising obstetric concerns which are now becoming a new research field. The growing trend of advanced maternal age can be attributed to the changes in women’s lifestyle and roles they play, and the development of advanced technology that aids in childbearing in multiparous women [16]. In China, to fight against the aging society challenge, the “one child one family” has been eliminated, and more families are making their decision to welcome the second child. However, women with advanced maternal age may have more obstetric complications and poorer obstetric outcomes compared with childbearing women under 35 years [17]. A meta-analysis of all the related studies found that the rate of stillbirth is increased in advanced maternal age pregnant women, and the risk increases with increased maternal age [18].
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The social and lifestyle changes are also occurring in the WWE population. However, the obstetric risks of WWE in the advanced maternal age have not been well studied. There is a growing need to understand the associated issues with advanced maternal age in WWE. In this study, we set out to explore the seizure control and obstetric complications of WWE in advanced maternal age.
Methods
The epilepsy pregnancy registry
The epilepsy pregnancy registry at West China Hospital was established in May 2014, and has been reviewed and approved by the ethics committee. It is a prospective registry based on epilepsy clinic [19]. Women diagnosed with epilepsy at childbearing age were asked to give written informed consent to participate in the registry and renew their information every 3 months at each clinical visit. The entire follow-up included clinical follow-up every 3 months at the outpatient clinic till the delivery, and a final follow-up 1 year thereafter. A management team including experienced epileptologists also checked the status and visits of patients. If a patient missed a clinical visit, they would contact the patient by telephone to collect information.
Each patient was assigned forms A–E, corresponding to different types of information in various periods during pregnancy. Form A contained basic demographic information (maternal age, education level, place of residence, employment status, marital status), obstetric information (date of last menstrual period, pregnancy plan, and reproductive history), information of epilepsy (duration of epilepsy, epilepsy type, seizure type, baseline seizure frequency before pregnancy, and usage of ASM). Form B documented information in the first trimester, including substance and ASMs exposure, complications, use of folate acid, medical exanimation findings and epilepsy management. Forms C and D documented the same information as in form B in the mid- and last trimesters separately. Form D contained delivery information at labor and fetus evaluation at birth. Form E was finished 1 year after birth, focusing on the complications and seizure control after birth, with extra information on breastfeeding, infant growth, malformations, and disease profile.
Patient selection
Patients starting their pregnancy at the age of 35 or older (according to the date of the last menstrual period before pregnancy) were selected from the registry database. Information of each patient was carefully reviewed. Patients with information available at all three trimesters were included.
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All the data were processed by IBM SPSS version 22.0. The demographic characteristics, seizure frequency, treatment change, obstetric complications, and outcomes were described with ratio.
Results
Demographics and obstetric features
After removing duplicate records and records with incomplete information in the trimesters, 15 women were finally included in this study. Their average age at pregnancy was 36.32 ± 2.39 years, and over half (53.33%) of them had a college degree and a stable job.
The majority of them (11/15, 73.33%) were primiparas, four of them (26.67%) were pluriparous, and 12 (80%) had a history of abortion, mostly more than once. One patient was in gemellary pregnancy. The most common reasons for abortion are societal factors, followed by medical considerations like possibilities of heredity/medication-caused obstetric complications and abnormal pregnancy (extrauterine pregnancy and pregnancy with an intrauterine device). All the four pluriparous women had vaginal delivery for their first child with no obstetric complications, and all the first children were healthy.
Seizure frequency during pregnancy
Seven patients (46.67%) had two different seizure manifestations before pregnancy. The seizures included focal bilateral tonic-clonic seizures (54.55%), generalized tonic-clonic seizures (22.73%), and focal impaired awareness seizures (18.18%). The seizure types remained unchanged in each patient, and no new seizure types were documented during the pregnancy.
Combining the seizure types together, the seizure frequency was most common at the monthly level, with two patients having focal impaired awareness seizures several times a day. Nine patients had active epilepsy, two were stable, and four withdrew their ASM under surveillance before pregnancy.
The patients with active epilepsy still had seizures during pregnancy. However, the frequency of seizures changed over time (Table 1), except for one patient who had seizures as the same frequency as previous. The frequency of tonic-clonic seizures increased from yearly level (88.89%) before pregnancy and at the first trimester to quarterly level at the mid (77.78%) and last trimesters (55.56%). The patients with stable disease and ASM withdrawal were generally uneventful, but there was one patient having a tonic-clonic seizure at the last trimester, which directly caused premature delivery with precipitate labor. No status epilepticus was documented for any patient.
Table. 1
Changes of ASM and seizure frequency during different trimesters
NO. | ASM before pregnancy | Seizure frequency before pregnancy | ASM changes in the 1st trimester | ASM changes in the 2nd trimester | ASM changes in the 3rd trimester | Seizure frequency change in the 1st trimester | Seizure frequency change in the 2nd trimester | Seizure frequency change in the 3rd trimester |
|---|---|---|---|---|---|---|---|---|
1 | VPA | Yearly | Stop ASM | VPA resumed | Increased | Increased | ||
2 | PHT | Monthly | Stop ASM | PHT resumed | Increased | Increased | Increased | |
3 | CBZ | More than 1 year | ||||||
4 | LEV | Monthly | Stop ASM | LEV resumed | Increased | Increased | ||
5 | More than 1 year | |||||||
6 | OXC, LEV | Monthly | Decreased | Decreased | ||||
7 | More than 1 year | |||||||
8 | More than 1 year | |||||||
9 | LEV | Monthly | Stop ASM | Decreased | ||||
10 | TPM | More than 1 year | TPM dose decrease | |||||
11 | CBZ, LEV | Daily | Increased | Decreased | ||||
12 | CBZ, LEV | Daily | Increased | Decreased | ||||
13 | More than 1 year | Increased | ||||||
14 | LTG, LEV | Monthly | LTG dose increase | LEV dose increase | LTG dose increase | Increased | Increased | Increased |
15 | TPM, PHT | Monthly | PHT → LTG | TPM → LEV |
Treatment changes during pregnancy
Before pregnancy, six patients were on monotherapy, five on polytherapy (four having two medications and one having three medications), and four under no medication (seizure free, therefore standard ASM withdrawal was applied). The monotherapy included levetiracetam (LEV), carbamazepine (CBZ), topiramate (TPM), and sodium valproate (VPA), preferably LEV (Table 1).
Treatment changed in the group of active epilepsy. Four out of the nine patients stopped medications by themselves to avoid the assumed adverse effects on the fetus. Three resumed their previous drug regimen after visits to epileptologists. One patient was off-medicine during the whole pregnancy, and no increase in seizure frequency was documented for that patient. One patient increased dosage of Lamotrigine in her polytherapy regimen during the first trimester, and then eventually increased dosage of LEV in mid-trimester and Lamotrigine in the last trimester for better seizure control.
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Obstetric complications during pregnancy
Among the 15 patients, 3 had vaginal bleeding in the first trimester, and one had slight elevations of glucose, protein and acetone bodies in the urine but these returned to normal on a re-check 2 weeks later.
Two patients had hypothyroidism at the mid-trimester and were on thyroxine supplement thereafter. One had anemia and was on regular treatment with re-check as well. Six patients had abnormal fetus ultrasound during the mid-trimester, four were found to have circular of the umbilical cord, and two showed slightly abnormal fetal growth compared to the reference.
There were also complications at the last trimester. Two patients had pre-eclampsia together with other accompanying conditions: gestational diabetes, and intrahepatic cholestasis, respectively. The patient with pre-eclampsia and intrahepatic cholestasis was found with fetal distress in the uterus, and had a premature delivery with third-degree amniotic fluid pollution. Other complications included intrahepatic cholestasis in one patient, and premature delivery with precipitate labor after a tonic-clonic seizure in one patient as stated above.
The data of delivery details were available for 13 patients, including 11 receving Caesarean section, and 2 of vaginal delivery. The Caesarean section was conducted due to the complications at the trimesters or during delivery (e.g., protracted active phase) in 7 patients, following obstetrician’s advice in 2 patients, and as to the demand of patients and their families in 2 patients. The average birth weight was 3,142.50 ± 670.45 g; the APGAR (Activity, Pulse, Grimace, Appearance, Respiration) grade ranged 7–10 points for all the patients. Two babies born at low birth weight were documented as 2,170 g and 2,000 g, both being premature deliveries.
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Discussion
In this preliminary study, the 15 WWE of advanced maternal age had similar seizure frequency changes as reported data on the general WWE [2, 3], but more complications during pregnancy and delivery compared to the general WWE [4].
All patients in this study were above 35 years at pregnancy, with an average age of 36.32 years. A majority (73.33%) of them were primiparas and the experience of abortion reflected their concerns about the disease, its potential influence on their offspring, and the adverse effects of ASM. Half of them had a college level or above and a stable job and income, indicating that this particular group of pregnant WWE had a specific lifestyle and role.
Previous studies have shown that, although the seizure frequency changes during pregnancy, the pattern of change is unclear and there is no decisive conclusion on whether the seizure burden is increased or decreased [2, 3]. Here, we found that the increase of seizure frequency in the mid-trimester seemed more obvious than in other periods and was related to the increase in tonic-clonic seizures. Most of our patients had tonic-clonic seizures at a yearly level before pregnancy, and the frequency dramatically increased to a quarterly level in mid-trimester and continued till the last trimester. Mawer G et al. found that there are fewer women having convulsive seizures during the second half of pregnancy (21 weeks to term) than in the first 20 weeks. However, this rule does not apply to those on Lamotrigine or polytherapy [5]. Differently, in this study we compared the seizure frequency changes by trimesters, and did not find a trend of decrease in later pregnancy, neither was there any relationship with the influence of Lamotrigine and polytherapy. This may be due to the hormonal changes or drug concentration changes induced by them. Therefore, studies employing larger numbers of patients are needed to validate the phenomenon and clarify the underlying mechanisms of seizure frequency change during pregnancy.
Better control of seizures in patients with active epilepsy has always been the focus of our work. Consistent with previous studies, the majority of WWE were under monotherapy during pregnancy [2, 3]. Four patients stopped their medication when found pregnant. These patients need to be educated to stay on their drugs and never withdraw ASM by themselves. Educational programs should emphasize the benefits of continuing medication while notifying them the side effects as well. Meanwhile, for patients on stable epilepsy or already off their ASM, they also need to understand the risk of relapse and be notified to avoid certain factors that could induce seizure onset. In our study, one patient without ASM had a seizure reoccurrence, which caused premature delivery with precipitate labor.
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Although there was no controlled group in our study, the obstetric complications during all the trimesters were common in this small sample, including vaginal bleeding, hypothyroidism, anemia, and pre-eclampsia. These complications have been reported previously in other studies, with a higher risk occurring in WWE especially those on medications during pregnancy [4, 5]. In particular, patients in current study showed pre-eclampsia complicated with other conditions like gestational diabetes and intrahepatic cholestasis. The caesarean section rate was also high in our patients, mainly due to the complications occurring at trimesters or during delivery.
Conclusions
In conclusion, in this preliminary study of advanced maternal age and WWE, although the sample size was small and no control group was included, the results demonstrated common obstetric complications in WWE of advanced maternal age. Future studies with controls and large sample sizes are needed to further illustrate the phenomenon we observed from the 15 patients.
Acknowledgements
We thank all the colleagues previously worked or currently working on the epilepsy pregnancy registry of West China Hospital.
Declarations
Ethics approval and consent to participate
This study was approved by the Ethics Committee of West China Hospital, Sichuan University. Written informed consent was obtained from all the individuals enrolled in this study.
Consent for publication
The informed consent about publication was obtained from the patients.
Competing interests
Author Dong Zhou is a member of the Editorial Board for Acta Epileptologica. Author Dong Zhou was not involved in the journal’s review of, or decisions related to this manuscript.
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